Facile synthesis of (2R, 3R)-phenylalanine-2,3-d2 and its application to conformational analysis of gramicidin S
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Labelling of aromatic amino-acids stereoselectively with tritium in the β-methylene group: the stereochemistry of hydroxylation in the biosynthesis of haemanthamine
2. Conformational analysis of amino acids and peptides using specific isotope substitution. II. Conformation of serine, tyrosine, phenylalanine, aspartic acid, asparagine, and aspartic acid .beta.-methyl ester in various ionization states
3. Simultaneous synthesis of both diastereomers of stereoselectively β-deuterated phenylalanines: (2S,3R)- and (2R,3R)-PhCHDCH(NH2)COOH
4. Asymmetric hydrogenation of .alpha.,.beta.-dehydroamino acid residue in cyclic dipeptides
5. CYCLIC PEPTIDES
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Efficient and Selective Deuteration of Phenylalanine Derivatives Catalyzed by Pd/C;Synlett;2005
2. Asymmetric hydrogenations of diketopiperazines;Topics in Catalysis;2000
3. Facile Synthesis of (2R,3R)-Phenylalanine-2,3-d2and NMR Study on Deuterated Gramicidin S;Bulletin of the Chemical Society of Japan;1984-08
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